Yu Mei-Hui, Space Brian, Franz Douglas, Zhou Wei, He Chaohui, Li Libo, Krishna Rajamani, Chang Ze, Li Wei, Hu Tong-Liang, Bu Xian-He
School of Materials Science and Engineering, National Institute for Advanced Materials , Nankai University , Tianjin 300350 , China.
Department of Chemistry , University of South Florida , 4202 East Fowler Avenue , Tampa , Florida 33620 , United States.
J Am Chem Soc. 2019 Nov 6;141(44):17703-17712. doi: 10.1021/jacs.9b07807. Epub 2019 Oct 22.
Physical adsorption of gas molecules in microporous materials is an exothermic process, with desorption entropy driving a decrease in uptake with temperature. Enhanced gas sorption with increasing temperature is rare in porous materials and is indicative of sorbate initiated structural change. Here, sorption of CH, CH, and CH in a flexible microporous metal-organic framework (MOF) {Cu(FPBDC)]·DMF} () (HFPBDC = 5-(5-fluoropyridin-3-yl)-1,3-benzenedicarboxylic acid) that increases with rising temperature over a practically useful temperature and pressure range is reported along with other small molecule and hydrocarbon sorption isotherms. Single X-ray diffraction studies, temperature-dependent gas sorption isotherms, and variable temperature powder X-ray diffraction experiments, and electronic structure calculations were performed to characterize the conformation-dependent sorption behavior in . In total, the data supports that the atypical sorption behavior is a result of loading-dependent structural changes in the flexible framework of induced by sorbate-specific guest-framework interactions. The sorbates cause subtle adaptations of the framework distinct to each sorbate providing an induced-fit separation mechanism to resolve chemically similar hydrocarbons through highly specific sorbate-sorbent interactions. The relevant intermolecular contacts are shown to be predominantly repulsion and dispersion interactions. is also found to be stable in aqueous solutions including toleration of pH changes. These experiments demonstrate the potential of this flexible microporous MOF for cost and energy efficient industrial hydrocarbon separation and purification processes. The efficacy for the separation of CH/CH mixtures is explicitly demonstrated using (i.e., activated ) for a particular useful temperature range.
气体分子在微孔材料中的物理吸附是一个放热过程,解吸熵导致吸附量随温度降低。在多孔材料中,随着温度升高气体吸附增强的情况很少见,这表明吸附质引发了结构变化。本文报道了在一种柔性微孔金属有机框架(MOF){Cu(FPBDC)]·DMF}()(HFPBDC = 5-(5-氟吡啶-3-基)-1,3-苯二甲酸)中,CH、CH和CH的吸附量在实际有用的温度和压力范围内随温度升高而增加,同时还报道了其他小分子和烃类的吸附等温线。进行了单晶X射线衍射研究、温度依赖性气体吸附等温线、变温粉末X射线衍射实验以及电子结构计算,以表征中的构象依赖性吸附行为。总体而言,数据支持这种非典型吸附行为是由吸附质特异性客体-框架相互作用引起的柔性框架中负载依赖性结构变化的结果。吸附质会导致框架发生细微的适应性变化,每种吸附质都不同,从而提供了一种诱导契合分离机制,通过高度特异性的吸附质-吸附剂相互作用来分离化学性质相似的烃类。相关的分子间接触主要表现为排斥和色散相互作用。还发现其在水溶液中稳定,包括对pH变化的耐受性。这些实验证明了这种柔性微孔MOF在经济高效的工业烃类分离和纯化过程中的潜力。在特定的有用温度范围内,使用(即活化的)明确证明了其对CH/CH混合物的分离效果。